The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126476381 12647638 1 I 20160715 0 20160811 20160811 DIR 41.37 YR F N 148.40000 KG 20160809 N US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126476381 12647638 1 PS MERCAPTOPURINE. MERCAPTOPURINE 1 0 1400 MG
126476381 12647638 2 SS METHOTREXATE. METHOTREXATE 1 0 200 MG
126476381 12647638 4 SS PREDNISONE. PREDNISONE 1 0 800 MG
126476381 12647638 6 SS VINCRISTINE SULFATE. VINCRISTINE SULFATE 1 0 2 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126476381 12647638 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126476381 12647638 Acute lymphocytic leukaemia recurrent
126476381 12647638 Atelectasis
126476381 12647638 Depression
126476381 12647638 Hyperbilirubinaemia
126476381 12647638 Insomnia
126476381 12647638 Nausea
126476381 12647638 Pneumonitis
126476381 12647638 Pyrexia
126476381 12647638 Splenomegaly
126476381 12647638 Vomiting

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126476381 12647638 1 20160502 0
126476381 12647638 2 20160502 0
126476381 12647638 4 20160506 0
126476381 12647638 6 20160502 0